ASUC chem 15 - CHEMISTRY 3B Professor Peter Vollhardt...

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CHEMISTRY 3B Professor Peter Vollhardt 10/16/08 Lecture 15 ASUC Lecture Notes Online is the only authorized note-taking service at UC Berkeley. Do not share, copy or illegally distribute (electronically or otherwise) these notes. Our student-run program depends on your individual subscription for its continued existence. These notes are copyrighted by the University of California and are for your personal use only. D O N O T C O P Y Sharing or copying these notes is illegal and could end note taking for this course. LECTURE Reactions Reactions involving the carbonyl function lead to carboxylic acid derivatives: Nucleophilic substitution occurs by addition- elimination. Nucleophilic substitution by addition-elimination Base catalyzed mechanism: Acid catalyzed mechanism: Synthesis of carboxylic acid derivatives A. Alkanoyl Halides: In order to create these acyl halides, we use reagents other than halide ions, namely SOCl 2 , PCl 5 , and PBr 3 .
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This note was uploaded on 10/07/2010 for the course CHEM 3b taught by Professor Pederson during the Fall '08 term at University of California, Berkeley.

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ASUC chem 15 - CHEMISTRY 3B Professor Peter Vollhardt...

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